Anderson Robert F.

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Anderson

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Robert F.

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0000-0002-8472-2494

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Comparing glacial and Holocene opal fluxes in the Pacific sector of the Southern Ocean

(American Geophysical Union, 2009-06-03) Bradtmiller, Louisa I. ; Anderson, Robert F. ; Fleisher, Martin Q. ; Burckle, Lloyd H.

The silicic acid leakage hypothesis (SALH) predicts that during glacial periods excess silicic acid was transported from the Southern Ocean to lower latitudes, which favored diatom production over coccolithophorid production and caused a drawdown of atmospheric CO2. Downcore records of 230Th-normalized opal (biogenic silica) fluxes from 31 cores in the Pacific sector of the Southern Ocean were used to compare diatom productivity during the last glacial period to that of the Holocene and to examine the evidence for increased glacial Si export to the tropics. Average glacial opal fluxes south of the modern Antarctic Polar Front (APF) were less than during the Holocene, while average glacial opal fluxes north of the APF were greater than during the Holocene. However, the magnitude of the increase north of the APF was not enough to offset decreased fluxes to the south, resulting in a decrease in opal burial in the Pacific sector of the Southern Ocean during the last glacial period, equivalent to approximately 15 Gt opal ka−1. This is consistent with the work of Chase et al. (2003a), and satisfies the primary requirement of the SALH, assuming that the upwelled supply of Si was approximately equivalent during the Holocene and the glacial period. However, previous results from the equatorial oceans are inconsistent with the other predictions of the SALH, namely that either the Corg:CaCO3 ratio or the rate of opal burial should have increased during glacial periods. We compare the magnitudes of changes in the Southern Ocean and the tropics and suggest that Si escaping the glacial Southern Ocean must have had an alternate destination, possibly the continental margins. There is currently insufficient data to test this hypothesis, but the existence of this sink and its potential impact on glacial pCO2 remain interesting topics for future study.
Trace metal evidence for deglacial ventilation of the abyssal Pacific and Southern Oceans

(American Geophysical Union, 2021-08-17) Pavia, Frank ; Wang, Shouyi ; Middleton, Jennifer L. ; Murray, Richard W. ; Anderson, Robert F.

The deep ocean has long been recognized as the reservoir that stores the carbon dioxide (CO2) removed from the atmosphere during Pleistocene glacial periods. The removal of glacial atmospheric CO2 into the ocean is likely modulated by an increase in the degree of utilization of macronutrients at the sea surface and enhanced storage of respired CO2 in the deep ocean, known as enhanced efficiency of the biological pump. Enhanced biological pump efficiency during glacial periods is most easily documented in the deep ocean using proxies for oxygen concentrations, which are directly linked to respiratory CO2 levels. We document the enhanced storage of respired CO2 during the Last Glacial Maximum (LGM) in the Pacific Southern Ocean and deepest Equatorial Pacific using records of deglacial authigenic manganese, which form as relict peaks during increases in bottom water oxygen (BWO) concentration. These peaks are found at depths and regions where other oxygenation histories have been ambiguous, due to diagenetic alteration of authigenic uranium, another proxy for BWO. Our results require that the entirety of the abyssal Pacific below approximately 1,000 m was enriched in respired CO2 and depleted in oxygen during the LGM. The presence of authigenic Mn enrichment in the deep Equatorial Pacific for each of the last five deglaciations suggests that the storage of respired CO2 in the deep ocean is a ubiquitous feature of late-Pleistocene ice ages.
Evidence of silicic acid leakage to the tropical Atlantic via Antarctic Intermediate Water during Marine Isotope Stage 4

(John Wiley & Sons, 2013-06-27) Griffiths, James D. ; Barker, Stephen ; Hendry, Katharine R. ; Thornalley, David J. R. ; van de Flierdt, Tina ; Hall, Ian R. ; Anderson, Robert F.

Antarctic Intermediate Water (AAIW) and Subantarctic Mode Water (SAMW) are the main conduits for the supply of dissolved silicon (silicic acid) from the deep Southern Ocean (SO) to the low-latitude surface ocean and therefore have an important control on low-latitude diatom productivity. Enhanced supply of silicic acid by AAIW (and SAMW) during glacial periods may have enabled tropical diatoms to outcompete carbonate-producing phytoplankton, decreasing the relative export of inorganic to organic carbon to the deep ocean and lowering atmospheric pCO2. This mechanism is known as the “silicic acid leakage hypothesis” (SALH). Here we present records of neodymium and silicon isotopes from the western tropical Atlantic that provide the first direct evidence of increased silicic acid leakage from the Southern Ocean to the tropical Atlantic within AAIW during glacial Marine Isotope Stage 4 (~60–70 ka). This leakage was approximately coeval with enhanced diatom export in the NW Atlantic and across the eastern equatorial Atlantic and provides support for the SALH as a contributor to CO2 drawdown during full glacial development.
Testing models of thorium and particle cycling in the ocean using data from station GT11-22 of the U.S. GEOTRACES North Atlantic section

( 2016-03-31) Lerner, Paul ; Marchal, Olivier ; Lam, Phoebe J. ; Anderson, Robert F. ; Buesseler, Ken O. ; Charette, Matthew A. ; Edwards, R. Lawrence ; Hayes, Christopher T. ; Huang, Kuo-Fang ; Lu, Yanbin ; Robinson, Laura F. ; Solow, Andrew R.

Thorium is a highly particle-reactive element that possesses different measurable radio-isotopes in seawater, with well-constrained production rates and very distinct half-lives. As a result, Th has emerged as a key tracer for the cycling of marine particles and of their chemical constituents, including particulate organic carbon. Here two different versions of a model of Th and particle cycling in the ocean are tested using an unprecedented data set from station GT11-22 of the U.S. GEOTRACES North Atlantic Section: (i) 21 228;230;234Th activities of dissolved and particulate fractions, (ii) 228Ra activities, (iii) 234;238U activities estimated from salinity data and an assumed 234U/238U ratio, and (iv) particle concentrations, below a depth of 125 m. The two model versions assume a single class of particles but rely on different assumptions about the rate parameters for sorption reactions and particle processes: a first version (V1) assumes vertically uniform parameters (a popular description), whereas the second (V2) does not. Both versions are tested by fitting to the GT11-22 data using generalized nonlinear least squares and by analyzing residuals normalized to the data errors. We find that model V2 displays a significantly better fit to the data than model V1. Thus, the mere allowance of vertical variations in the rate parameters can lead to a significantly better fit to the data, without the need to modify the structure or add any new processes to the model. To understand how the better fit is achieved we consider two parameters, K = k1=(k-1 + β-1) and K/P, where k1 is the adsorption rate constant, k-1 the desorption rate constant, β-1 the remineralization rate constant, and P the particle concentration. We find that the rate constant ratio K is large (≥0.2) in the upper 1000 m and decreases to a nearly uniform value of ca. 0.12 below 2000 m, implying that the specific rate at which Th attaches to particles relative to that at which it is released from particles is higher in the upper ocean than in the deep ocean. In contrast, K/P increases with depth below 500 m. The parameters K and K/P display significant positive and negative monotonic relationship with P, respectively, which is collectively consistent with a particle concentration effect.
Th-230 and Pa-231 on GEOTRACES GA03, the US GEOTRACES North Atlantic transect, and implications for modern and paleoceanographic chemical fluxes

( 2014-07) Hayes, Christopher T. ; Anderson, Robert F. ; Fleisher, Martin Q. ; Huang, Kuo-Fang ; Robinson, Laura F. ; Lu, Yanbin ; Cheng, Hai ; Edwards, R. Lawrence ; Moran, S. Bradley

The long-lived uranium decay products 230Th and 231Pa are widely used as quantitative tracers of adsorption to sinking particles (scavenging) in the ocean by exploiting the principles of radioactive disequilibria. Because of their preservation in the Pleistocene sediment record and through largely untested assumptions about their chemical behavior in the water column, the two radionuclides have also been used as proxies for a variety of chemical fluxes in the past ocean. This includes the vertical flux of particulate matter to the seafloor, the lateral flux of insoluble elements to continental margins (boundary scavenging), and the southward flux of water out of the deep North Atlantic. In a section of unprecedented vertical and zonal resolution, the distributions of 230Th and 231Pa across the North Atlantic shed light on the marine cycling of these radionuclides and further inform their use as tracers of chemical flux. Enhanced scavenging intensities are observed in benthic layers of resuspended sediments on the eastern and western margins and in a hydrothermal plume emanating from the Mid-Atlantic Ridge. Boundary scavenging is clearly expressed in the water column along a transect between Mauritania and Cape Verde which is used to quantify a bias in sediment fluxes calculated using 230Th-normalization and to demonstrate enhanced 231Pa removal from the deep North Atlantic by this mechanism. The influence of deep ocean ventilation that leads to the southward export of 231Pa is apparent. The 231Pa/230Th ratio, however, predominantly reflects spatial variability in scavenging intensity, complicating its applicability as a proxy for the Atlantic meridional overturning circulation.
Concentrations of size-fractionated particulate thorium and protactinium isotopes (Th-232, Th-230, Pa-231) in seawater collected during the U.S. GEOTRACES Arctic cruise (HLY1502, GN01) on USCGC Healy from August to October 2015

(Biological and Chemical Oceanography Data Management Office (BCO-DMO). Contact: bco-dmo-data@whoi.edu, 2022-05-13) Vivancos, Sebastian M. ; Anderson, Robert F. ; Fleisher, Martin Q. ; Zhang, Pu ; Li, Xianglei ; Edwards, R. Lawrence ; Cheng, Hai

This dataset contains concentrations of size-fractionated particulate thorium and protactinium isotopes (Th-232, Th-230, Pa-231) in seawater collected during the U.S. GEOTRACES Arctic cruise (HLY1502, GN01) on USCGC Healy from August to October 2015. This is compiled data produced by two laboratories with the following associations: Lamont-Doherty Earth Observatory of Columbia University (LDEO) and the University of Minnesota (UMN). All data have been deemed intercalibrated by the International GEOTRACES Standards and Intercalibration (S&I) Committee. For a complete list of measurements, refer to the full dataset description in the supplemental file 'Dataset_description.pdf'. The most current version of this dataset is available at: https://www.bco-dmo.org/dataset/834741
Depth profiles of seawater particulate 232Th, 230Th, and 231Pa from R/V Sonne cruise SO245 (UltraPac, GPpr09) during Dec 2015 to Jan 2016

(Biological and Chemical Oceanography Data Management Office (BCO-DMO). Contact: bco-dmo-data@whoi.edu, 2020-06-03) Anderson, Robert F. ; Fleisher, Martin Q.

This dataset contains depth profiles of seawater particulate 232Th, 230Th, and 231Pa from R/V Sonne cruise SO245 (UltraPac, GPpr09). For a complete list of measurements, refer to the full dataset description in the supplemental file 'Dataset_description.pdf'. The most current version of this dataset is available at: https://www.bco-dmo.org/dataset/813317
Concentrations of size-fractionated particulate thorium and protactinium isotopes (Th-232, Th-230, Pa-231) in seawater collected during the U.S. GEOTRACES Arctic cruise (HLY1502, GN01) on USCGC Healy from August to October 2015

(Biological and Chemical Oceanography Data Management Office (BCO-DMO). Contact: bco-dmo-data@whoi.edu, 2021-03-01) Vivancos, Sebastian M. ; Anderson, Robert F. ; Fleisher, Martin Q. ; Zhang, Pu ; Li, Xianglei ; Edwards, R. Lawrence ; Cheng, Hai

This dataset contains concentrations of size-fractionated particulate thorium and protactinium isotopes (Th-232, Th-230, Pa-231) in seawater collected during the U.S. GEOTRACES Arctic cruise (HLY1502, GN01) on USCGC Healy from August to October 2015. This is compiled data produced by two laboratories with the following associations: Lamont-Doherty Earth Observatory of Columbia University (LDEO) and the University of Minnesota (UMN). All data have been deemed intercalibrated by the International GEOTRACES Standards and Intercalibration (S&I) Committee. For a complete list of measurements, refer to the full dataset description in the supplemental file 'Dataset_description.pdf'. The most current version of this dataset is available at: https://www.bco-dmo.org/dataset/834741
Concentrations of dissolved thorium and protactinium isotopes (Th-232, Th-230, Pa-231) in seawater, sea ice, and melt ponds collected during the U.S. GEOTRACES Arctic cruise (HLY1502, GN01) on USCGC Healy from August to October 2015

(Biological and Chemical Oceanography Data Management Office (BCO-DMO). Contact: bco-dmo-data@whoi.edu, 2021-02-26) Vivancos, Sebastian M. ; Anderson, Robert F. ; Fleisher, Martin Q. ; Zhang, Pu ; Li, Xianglei ; Edwards, R. Lawrence ; Cheng, Hai

This dataset contains concentrations of dissolved thorium and protactinium isotopes (Th-232, Th-230, Pa-231) in seawater, sea ice, and melt ponds collected during the U.S. GEOTRACES Arctic cruise (HLY1502, GN01) on USCGC Healy from August to October 2015. This is compiled data produced by two laboratories with the following associations: Lamont-Doherty Earth Observatory of Columbia University (LDEO) and the University of Minnesota (UMN). All data have been deemed intercalibrated by the International GEOTRACES Standards and Intercalibration (S&I) Committee. For a complete list of measurements, refer to the full dataset description in the supplemental file 'Dataset_description.pdf'. The most current version of this dataset is available at: https://www.bco-dmo.org/dataset/833887
Actinium and radium fluxes from the seabed in the northeast Pacific Basin

(Elsevier, 2022-10-22) Kemnitz, Nathaniel ; Hammond, Douglas E. ; Henderson, Paul ; Le Roy, Emilie ; Charette, Matthew ; Moore, Willard ; Anderson, Robert F. ; Fleisher, Martin Q. ; Leal, Anne ; Black, Erin ; Hayes, Christopher T. ; Adkins, Jess ; Berelson, William ; Bian, Xiaopeng

Five sediment cores were collected along a cruise tract from Hawaii to Alaska in August 2017 (C-Disk-IV cruise) with the objective of characterizing the behavior of 227Ac, 228Ra, and 226Ra and their fluxes into the overlying water column, information that is essential to the interpretation of the distribution of these tracers in the ocean, for example, as measured on GEOTRACES cruises. Solid phase profiles of these isotopes were measured, and reaction-transport models were applied that incorporated molecular diffusion, bioturbation, sedimentation, distribution coefficients (kd), and the fraction of each isotope released to pore water by parent decay (called F). Fits to these profiles used kd values determined in lab experiments for C-Disk-IV sediments. Ra kd values (1000–3000 mL g−1) agreed with previous estimates for deep-sea sediments, and Ac kd values (3500–22,000 mL g−1) correlated with those for Ra but were about 7 times greater. Two independent approaches were used to quantify the benthic fluxes of 227Ac and 228Ra in the Northeast Pacific: (1) use of solid phase profiles with a reaction-transport model, as well as integrated downcore daughter-parent deficiency; and (2) direct measurement of fluxes based on core incubation. The two independent methods agreed within uncertainty, and the average 227Ac and 228Ra sediment fluxes for the Northeast Pacific are 90 ± 20 and 600 ± 200 dpm m−2-yr−1, respectively. The 226Ra sediment flux was only determined by the former approach, and the flux calculated in this study is similar to previous work in the North Pacific, averaging 1300 ± 200 dpm m−2-yr−1. This is over 2× higher than the water column inventory of 226Ra in this region (600 dpm m−2-yr−1), and indicates the importance of lateral 226Ra export from the N. Pacific. The largest 227Ac and Ra isotope fluxes in the study area are near the center of the Northeast Pacific (∼37°N). Smaller 227Ac, 228Ra and 226Ra fluxes occur north of 40°N, primarily due to dilution of their Pa and Th ancestors by higher sediment accumulation rates.
Comment on “Do geochemical estimates of sediment focusing pass the sediment test in the equatorial Pacific?” by M. Lyle et al.

(American Geophysical Union, 2007-03-06) Francois, Roger ; Frank, Martin ; Rutgers van der Loeff, Michiel M. ; Bacon, Michael P. ; Geibert, Walter ; Kienast, Stephanie S. ; Anderson, Robert F. ; Bradtmiller, Louisa I. ; Chase, Zanna ; Henderson, Gideon M. ; Marcantonio, Franco ; Allen, Susan E.
GEOTRACES intercalibration of 230Th, 232Th, 231Pa, and prospects for 10Be

(Association for the Sciences of Limnology and Oceanography, 2012-04) Anderson, Robert F. ; Fleisher, Martin Q. ; Robinson, Laura F. ; Edwards, R. Lawrence ; Hoff, John A. ; Moran, S. Bradley ; Rutgers van der Loeff, Michiel M. ; Thomas, Alexander L. ; Roy-Barman, Matthieu ; Francois, Roger

Nineteen labs representing nine nations participated in the GEOTRACES intercalibration initiative that determined concentrations of 232Th, 230Th, 231Pa, or 10Be in seawater, suspended particles or sediments. Results generally demonstrated good agreement among labs that analyzed marine sediments. Two sets of seawater samples, aliquots of particulate material filtered in situ, and/or aliquots of biogenic sediments were distributed to participating labs. Internal consistency among participating labs improved substantially between the first and second set of seawater samples. Contamination was a serious problem for 232Th. Standard Niskin bottles introduced no detectable contamination, whereas sample containers, reagents, and labware were implicated as sources of contamination. No detectable differences in concentrations of dissolved 232Th, 230Th, or 231Pa were observed among samples of seawater filtered through Nuclepore, Supor, or QMA (quartz) filters with pore diameters ranging between 0.4 and 1.0 μm. Isotope yield monitors equilibrate with dissolved Th in seawater on a time scale of much less than 1 day. Samples of filtered seawater acidified to a pH between 1.7 and 1.8 experienced no detectable loss of dissolved Th or Pa during storage for up to 3 years. The Bermuda Atlantic Time Series station will serve as a GEOTRACES baseline station for future intercalibration of 232Th and 230Th concentrations in seawater. Efforts to improve blanks and standard calibration are ongoing, as is the development of methods to determine concentrations of particulate nuclides, tests of different filtration methods, and an increasing awareness of the need to define protocols for reporting uncertainties.
Improvements to 232-thorium, 230-thorium, and 231- protactinium analysis in seawater arising from GEOTRACES intercalibration

(Association for the Sciences of Limnology and Oceanography, 2012-07) Auro, Maureen E. ; Robinson, Laura F. ; Burke, Andrea ; Bradtmiller, Louisa I. ; Fleisher, Martin Q. ; Anderson, Robert F.

The GEOTRACES program requires the analysis of large numbers of seawater samples for 232Th, 230Th, and 231Pa. During the GEOTRACES international intercalibration exercise, we encountered unexpected difficulties with recovery and contamination of these isotopes, 232Th in particular. Experiments were carried out to identify the source of these issues, leading to a more streamlined and efficient procedure. The two particular problems that we identified and corrected were (1) frits in columns supplied by Bio-Rad Laboratories caused loss of Th during column chemistry and (2) new batches of AG1-X8 resin supplied by Bio-Rad Laboratories released more than 100 pg of 232Th during elution of sample. To improve yields and blanks, we implemented a series of changes including switching to Eichrom anion exchange resin (100-200 μm mesh) and Environmental Express columns. All Th and Pa samples were analyzed on a Neptune multi-collector inductively-coupled-plasma mass spectrometer (MC-ICP-MS) using peak hopping of 230Th and 229Th on the central SEM, with either 232Th, 236U (or both) used to monitor for beam intensity. We used in-house laboratory standards to check for machine reproducibility, and the GEOTRACES intercalibration standard to check for accuracy. Over a 1-y period, the 2 s.d. reproducibility on the GEOTRACES SW STD 2010-1 was 2.5% for 230Th, 1.8% for 232Th, and 4% for 231Pa. The lessons learned during this intercalibration process will be of value to those analyzing U-Th-Pa and rare earth elements as part of the GEOTRACES program as well as those using U-series elements in other applications that require high yields and low blanks, such as geochronology.
Intensity of Th and Pa scavenging partitioned by particle chemistry in the North Atlantic Ocean

( 2015-01) Hayes, Christopher T. ; Anderson, Robert F. ; Fleisher, Martin Q. ; Vivancos, Sebastian M. ; Lam, Phoebe J. ; Ohnemus, Daniel C. ; Huang, Kuo-Fang ; Robinson, Laura F. ; Lu, Yanbin ; Cheng, Hai ; Edwards, R. Lawrence ; Moran, S. Bradley

The natural radionuclides 231Pa and 230Th are incorporated into the marine sediment record by scavenging, or adsorption to various particle types, via chemical reactions that are not fully understood. Because these isotopes have potential value in tracing several oceanographic processes, we investigate the nature of scavenging using trans-Atlantic measurements of dissolved (<0.45 μm) and particulate (0.8-51 μm) 231Pa and 230Th, together with major particle composition. We find widespread impact of intense scavenging by authigenic Fe/Mn (hydr)oxides, in the form of hydrothermal particles emanating from the Mid-Atlantic ridge and particles resuspended from reducing conditions near the seafloor off the coast of West Africa. Biogenic opal was not found to be a significant scavenging phase for either element in this sample set, essentially because of its low abundance and small dynamic range at the studied sites. Distribution coefficients in shallow (< 200 m) depths are anomalously low which suggests either the unexpected result of a low scavenging intensity for organic matter or that, in water masses containing abundant organic-rich particles, a greater percentage of radionuclides exist in the colloidal or complexed phase. In addition to particle concentration, the oceanic distribution of particle types likely plays a significant role in the ultimate distribution of sedimentary 230Th and 231Pa.
Global ocean sediment composition and burial flux in the deep sea

(American Geophysical Union, 2021-03-21) Hayes, Christopher T. ; Costa, Kassandra M. ; Anderson, Robert F. ; Calvo, Eva ; Chase, Zanna ; Demina, Ludmila L. ; Dutay, Jean-Claude ; German, Christopher R. ; Heimbürger, Lars-Eric ; Jaccard, Samuel L. ; Jacobel, Allison W. ; Kohfeld, Karen E. ; Kravchishina, Marina ; Lippold, Jörg ; Mekik, Figen ; Missiaen, Lise ; Pavia, Frank ; Paytan, Adina ; Pedrosa-Pamies, Rut ; Petrova, Mariia V. ; Rahman, Shaily ; Robinson, Laura F. ; Roy-Barman, Matthieu ; Sanchez-Vidal, Anna ; Shiller, Alan M. ; Tagliabue, Alessandro ; Tessin, Allyson C. ; van Hulten, Marco ; Zhang, Jing

Quantitative knowledge about the burial of sedimentary components at the seafloor has wide-ranging implications in ocean science, from global climate to continental weathering. The use of 230Th-normalized fluxes reduces uncertainties that many prior studies faced by accounting for the effects of sediment redistribution by bottom currents and minimizing the impact of age model uncertainty. Here we employ a recently compiled global data set of 230Th-normalized fluxes with an updated database of seafloor surface sediment composition to derive atlases of the deep-sea burial flux of calcium carbonate, biogenic opal, total organic carbon (TOC), nonbiogenic material, iron, mercury, and excess barium (Baxs). The spatial patterns of major component burial are mainly consistent with prior work, but the new quantitative estimates allow evaluations of deep-sea budgets. Our integrated deep-sea burial fluxes are 136 Tg C/yr CaCO3, 153 Tg Si/yr opal, 20Tg C/yr TOC, 220 Mg Hg/yr, and 2.6 Tg Baxs/yr. This opal flux is roughly a factor of 2 increase over previous estimates, with important implications for the global Si cycle. Sedimentary Fe fluxes reflect a mixture of sources including lithogenic material, hydrothermal inputs and authigenic phases. The fluxes of some commonly used paleo-productivity proxies (TOC, biogenic opal, and Baxs) are not well-correlated geographically with satellite-based productivity estimates. Our new compilation of sedimentary fluxes provides detailed regional and global information, which will help refine the understanding of sediment preservation.
The GEOTRACES Intermediate Data Product 2014

(Elsevier, 2015-04-16) Mawji, Edward ; Schlitzer, Reiner ; Dodas, Elena Masferrer ; Abadie, Cyril ; Abouchami, Wafa ; Anderson, Robert F. ; Baars, Oliver ; Bakker, Karel ; Baskaran, Mark ; Bates, Nicholas R. ; Bluhm, Katrin ; Bowie, Andrew R. ; Bown, Johann ; Boye, Marie ; Marie, Edward A. ; Branellec, Pierre ; Bruland, Kenneth W. ; Brzezinski, Mark A. ; Bucciarelli, Eva ; Buesseler, Ken O. ; Butler, Edward ; Cai, Pinghe ; Cardinal, Damien ; Casciotti, Karen L. ; Chaves, Joaquin E. ; Cheng, Hai ; Chever, Fanny ; Church, Thomas M. ; Colman, Albert S. ; Conway, Tim M. ; Croot, Peter L. ; Cutter, Gregory A. ; Baar, Hein J. W. de ; de Souza, Gregory F. ; Dehairs, Frank ; Deng, Feifei ; Dieu, Huong Thi ; Dulaquais, Gabriel ; Echegoyen-Sanz, Yolanda ; Edwards, R. Lawrence ; Fahrbach, Eberhard ; Fitzsimmons, Jessica N. ; Fleisher, Martin Q. ; Frank, Martin ; Friedrich, Jana ; Fripiat, Francois ; Galer, Stephen J. G. ; Gamo, Toshitaka ; Garcia Solsona, Ester ; Gerringa, Loes J. A. ; Godoy, Jose Marcus ; Gonzalez, Santiago ; Grossteffan, Emilie ; Hatta, Mariko ; Hayes, Christopher T. ; Heller, Maija Iris ; Henderson, Gideon M. ; Huang, Kuo-Fang ; Jeandel, Catherine ; Jenkins, William J. ; John, Seth G. ; Kenna, Timothy C. ; Klunder, Maarten ; Kretschmer, Sven ; Kumamoto, Yuichiro ; Laan, Patrick ; Labatut, Marie ; Lacan, Francois ; Lam, Phoebe J. ; Lannuzel, Delphine ; le Moigne, Frederique ; Lechtenfeld, Oliver J. ; Lohan, Maeve C. ; Lu, Yanbin ; Masqué, Pere ; McClain, Charles R. ; Measures, Christopher I. ; Middag, Rob ; Moffett, James W. ; Navidad, Alicia ; Nishioka, Jun ; Noble, Abigail E. ; Obata, Hajime ; Ohnemus, Daniel C. ; Owens, Stephanie A. ; Planchon, Frederic ; Pradoux, Catherine ; Puigcorbe, Viena ; Quay, Paul D. ; Radic, Amandine ; Rehkamper, Mark ; Remenyi, Tomas A. ; Rijkenberg, Micha J. A. ; Rintoul, Stephen R. ; Robinson, Laura F. ; Roeske, Tobias ; Rosenberg, Mark ; Rutgers van der Loeff, Michiel M. ; Ryabenko, Evgenia ; Saito, Mak A. ; Roshan, Saeed ; Salt, Lesley ; Sarthou, Geraldine ; Schauer, Ursula ; Scott, Peter M. ; Sedwick, Peter N. ; Sha, Lijuan ; Shiller, Alan M. ; Sigman, Daniel M. ; Smethie, William M. ; Smith, Geoffrey J. ; Sohrin, Yoshiki ; Speich, Sabrina ; Stichel, Torben ; Stutsman, Johnny ; Swift, James H. ; Tagliabue, Alessandro ; Thomas, Alexander L. ; Tsunogai, Urumu ; Twining, Benjamin S. ; van Aken, Hendrik M. ; van Heuven, Steven ; van Ooijen, Jan ; van Weerlee, Evaline ; Venchiarutti, Celia ; Voelker, Antje H. L. ; Wake, Bronwyn ; Warner, Mark J. ; Woodward, E. Malcolm S. ; Wu, Jingfeng ; Wyatt, Neil ; Yoshikawa, Hisayuki ; Zheng, Xin-Yuan ; Xue, Zichen ; Zieringer, Moritz ; Zimmer, Louise A.

The GEOTRACES Intermediate Data Product 2014 (IDP2014) is the first publicly available data product of the international GEOTRACES programme, and contains data measured and quality controlled before the end of 2013. It consists of two parts: (1) a compilation of digital data for more than 200 trace elements and isotopes (TEIs) as well as classical hydrographic parameters, and (2) the eGEOTRACES Electronic Atlas providing a strongly inter-linked on-line atlas including more than 300 section plots and 90 animated 3D scenes. The IDP2014 covers the Atlantic, Arctic, and Indian oceans, exhibiting highest data density in the Atlantic. The TEI data in the IDP2014 are quality controlled by careful assessment of intercalibration results and multi-laboratory data comparisons at cross-over stations. The digital data are provided in several formats, including ASCII spreadsheet, Excel spreadsheet, netCDF, and Ocean Data View collection. In addition to the actual data values the IDP2014 also contains data quality flags and 1-σ data error values where available. Quality flags and error values are useful for data filtering. Metadata about data originators, analytical methods and original publications related to the data are linked to the data in an easily accessible way. The eGEOTRACES Electronic Atlas is the visual representation of the IDP2014 data providing section plots and a new kind of animated 3D scenes. The basin-wide 3D scenes allow for viewing of data from many cruises at the same time, thereby providing quick overviews of large-scale tracer distributions. In addition, the 3D scenes provide geographical and bathymetric context that is crucial for the interpretation and assessment of observed tracer plumes, as well as for making inferences about controlling processes.
Flux of particulate elements in the North Atlantic Ocean constrained by multiple radionuclides

(American Geophysical Union, 2018-11-22) Hayes, Christopher T. ; Black, Erin E. ; Anderson, Robert F. ; Baskaran, Mark ; Buesseler, Ken O. ; Charette, Matthew A. ; Cheng, Hai ; Cochran, J. Kirk ; Edwards, R. Lawrence ; Fitzgerald, Patrick ; Lam, Phoebe J. ; Lu, Yanbin ; Morris, Stephanie O. ; Ohnemus, Daniel C. ; Pavia, Frank ; Stewart, Gillian ; Tang, Yi

Sinking particles strongly regulate the distribution of reactive chemical substances in the ocean, including particulate organic carbon and other elements (e.g., P, Cd, Mn, Cu, Co, Fe, Al, and 232Th). Yet, the sinking fluxes of trace elements have not been well described in the global ocean. The U.S. GEOTRACES campaign in the North Atlantic (GA03) offers the first data set in which the sinking flux of carbon and trace elements can be derived using four different radionuclide pairs (238U:234Th ;210Pb:210Po; 228Ra:228Th; and 234U:230Th) at stations co‐located with sediment trap fluxes for comparison. Particulate organic carbon, particulate P, and particulate Cd fluxes all decrease sharply with depth below the euphotic zone. Particulate Mn, Cu, and Co flux profiles display mixed behavior, some cases reflecting biotic remineralization, and other cases showing increased flux with depth. The latter may be related to either lateral input of lithogenic material or increased scavenging onto particles. Lastly, particulate Fe fluxes resemble fluxes of Al and 232Th, which all have increasing flux with depth, indicating a dominance of lithogenic flux at depth by resuspended sediment transported laterally to the study site. In comparing flux estimates derived using different isotope pairs, differences result from different timescales of integration and particle size fractionation effects. The range in flux estimates produced by different methods provides a robust constraint on the true removal fluxes, taking into consideration the independent uncertainties associated with each method. These estimates will be valuable targets for biogeochemical modeling and may also offer insight into particle sinking processes.
Dissolved and particulate barium distributions along the US GEOTRACES North Atlantic and East Pacific zonal transects (GA03 and GP16): global implications for the marine barium cycle

(American Geophysical Union, 2022-05-23) Rahman, Shaily ; Shiller, Alan M. ; Anderson, Robert F. ; Charette, Matthew A. ; Hayes, Christopher T. ; Gilbert, Melissa ; Grissom, Karen ; Lam, Phoebe J. ; Ohnemus, Daniel C. ; Pavia, Frank ; Twining, Benjamin S. ; Vivancos, Sebastian M.

Processes controlling dissolved barium (dBa) were investigated along the GEOTRACES GA03 North Atlantic and GP16 Eastern Tropical Pacific transects, which traversed similar physical and biogeochemical provinces. Dissolved Ba concentrations are lowest in surface waters (∼35–50 nmol kg−1) and increase to 70–80 and 140–150 nmol kg−1 in deep waters of the Atlantic and Pacific transects, respectively. Using water mass mixing models, we estimate conservative mixing that accounts for most of dBa variability in both transects. To examine nonconservative processes, particulate excess Ba (pBaxs) formation and dissolution rates were tracked by normalizing particulate excess 230Th activities. Th-normalized pBaxs fluxes, with barite as the likely phase, have subsurface maxima in the top 1,000 m (∼100–200 μmol m−2 year−1 average) in both basins. Barite precipitation depletes dBa within oxygen minimum zones from concentrations predicted by water mass mixing, whereas inputs from continental margins, particle dissolution in the water column, and benthic diffusive flux raise dBa above predications. Average pBaxs burial efficiencies along GA03 and GP16 are ∼37% and 17%–100%, respectively, and do not seem to be predicated on barite saturation indices in the overlying water column. Using published values, we reevaluate the global freshwater dBa river input as 6.6 ± 3.9 Gmol year−1. Estuarine mixing processes may add another 3–13 Gmol year−1. Dissolved Ba inputs from broad shallow continental margins, previously unaccounted for in global marine summaries, are substantial (∼17 Gmol year−1), exceeding terrestrial freshwater inputs. Revising river and shelf dBa inputs may help bring the marine Ba isotope budget more into balance.
230 Th normalization: new insights on an essential tool for quantifying sedimentary fluxes in the modern and quaternary ocean

(John Wiley & Sons, 2020-01-27) Costa, Kassandra M. ; Hayes, Christopher T. ; Anderson, Robert F. ; Pavia, Frank ; Bausch, Alexandra ; Deng, Feifei ; Dutay, Jean-Claude ; Geibert, Walter ; Heinze, Christoph ; Henderson, Gideon M. ; Hillaire‐Marcel, Claude ; Hoffmann, Sharon S. ; Jaccard, Samuel L. ; Jacobel, Allison W. ; Kienast, Stephanie S. ; Kipp, Lauren ; Lerner, Paul ; Lippold, Jörg ; Lund, David C. ; Marcantonio, Franco ; McGee, David ; McManus, Jerry F. ; Mekik, Figen ; Middleton, Jennifer L. ; Missiaen, Lise ; Not, Christelle ; Pichat, Sylvain ; Robinson, Laura F. ; Rowland, George H. ; Roy-Barman, Matthieu ; Tagliabue, Alessandro ; Torfstein, Adi ; Winckler, Gisela ; Zhou, Yuxin

230Th normalization is a valuable paleoceanographic tool for reconstructing high‐resolution sediment fluxes during the late Pleistocene (last ~500,000 years). As its application has expanded to ever more diverse marine environments, the nuances of 230Th systematics, with regard to particle type, particle size, lateral advective/diffusive redistribution, and other processes, have emerged. We synthesized over 1000 sedimentary records of 230Th from across the global ocean at two time slices, the late Holocene (0–5,000 years ago, or 0–5 ka) and the Last Glacial Maximum (18.5–23.5 ka), and investigated the spatial structure of 230Th‐normalized mass fluxes. On a global scale, sedimentary mass fluxes were significantly higher during the Last Glacial Maximum (1.79–2.17 g/cm2kyr, 95% confidence) relative to the Holocene (1.48–1.68 g/cm2kyr, 95% confidence). We then examined the potential confounding influences of boundary scavenging, nepheloid layers, hydrothermal scavenging, size‐dependent sediment fractionation, and carbonate dissolution on the efficacy of 230Th as a constant flux proxy. Anomalous 230Th behavior is sometimes observed proximal to hydrothermal ridges and in continental margins where high particle fluxes and steep continental slopes can lead to the combined effects of boundary scavenging and nepheloid interference. Notwithstanding these limitations, we found that 230Th normalization is a robust tool for determining sediment mass accumulation rates in the majority of pelagic marine settings (>1,000 m water depth).
Depth profiles of seawater dissolved 232Th, 230Th, and 231Pa from R/V Sonne cruise SO245 (UltraPac, GPpr09) during Dec 2015 to Jan 2016

(Biological and Chemical Oceanography Data Management Office (BCO-DMO). Contact: bco-dmo-data@whoi.edu, 2020-06-03) Anderson, Robert F. ; Fleisher, Martin Q.

This dataset contains depth profiles of seawater dissolved 232Th, 230Th, and 231Pa from R/V Sonne cruise SO245 (UltraPac, GPpr09). For a complete list of measurements, refer to the full dataset description in the supplemental file 'Dataset_description.pdf'. The most current version of this dataset is available at: https://www.bco-dmo.org/dataset/813133

Anderson Robert F.

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